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PRODUCT DETAIL

ALTUVOCT 500 IU prášok a rozpúšťadlo na injekčný roztok

Code 6664E
MA number EU/1/24/1824/002
Product Form: plv iol 1x500 IU + 3 ml solv. (liek.inj.skl. + striek.inj.napl.skl.)
MA Status: E - Valid centralised marketing authorisation
Type of procedure: EU Orphan
Therapeutic Class: 16 - ANTICOAGULANTIA (FIBRINOLYTICA, ANTIFIBRINOL.)
ATC:
B BLOOD AND BLOOD FORMING ORGANS
B02 ANTIHEMORRHAGICS
B02B LOCAL HEMOSTATICS, COMBINATIONS
B02BD Blood coagulation factors
B02BD02 Coagulation factor VIII
Shelf life: 48
Container: glass vial
Route of admin.: Intravenous use
Prescription Status: Medicinal product subject to restricted medical prescription.
Legal basis: Article 8(3) application - new active substance
MA issued: 17.06.2024
Validity: 17.06.2029
SmPC + PL: European Medicines Agency's database
Safety feature Yes
Data update: 25.06.2024
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